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Genetic evidence for facial variation being a composite phenotype of cranial variation and facial soft tissue thickness
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作者 Wei Qian Manfei Zhang +10 位作者 Kaiwen Wan Yunxia Xie Siyuan Du Jiarui Li Xiongzheng Mu Jiange Qiu Xiangyang Xue Xiahai Zhuang Yingzhi Wu Fan Liu Sijia Wang 《Journal of Genetics and Genomics》 SCIE CAS CSCD 2022年第10期934-942,共9页
Facial and cranial variation represent a multidimensional set of highly correlated and heritable phenotypes.Little is known about the genetic basis explaining this correlation.We develop a software package ALo SFL for... Facial and cranial variation represent a multidimensional set of highly correlated and heritable phenotypes.Little is known about the genetic basis explaining this correlation.We develop a software package ALo SFL for simultaneous localization of facial and cranial landmarks from head computed tomography(CT)images,apply it in the analysis of head CT images of 777 Han Chinese women,and obtain a set of phenotypes representing variation in face,skull and facial soft tissue thickness(FSTT).Association analysis of 301 single nucleotide polymorphisms(SNPs)from 191 distinct genomic loci previously associated with facial variation reveals an unexpected larger number of loci showing significant associations(P<1e-3)with cranial phenotypes than expected under the null(O/E=3.39),suggesting facial and cranial phenotypes share a substantial proportion of genetic components.Adding FSTT to a SNP-only model shows a large impact in explaining facial variance.A gene ontology analysis reveals that bone morphogenesis and osteoblast differentiation likely underlie our cranial-significant findings.Overall,this study simultaneously investigates the genetic effects on both facial and cranial variation of the same sample,supporting that facial variation is a composite phenotype of cranial variation and FSTT. 展开更多
关键词 facial variation Cranial variation Association analysis Single nucleotide polymorphism facial soft tissue thickness Computed tomography
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